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Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage

Human molecular genetics, 2007-10, Vol.16 (20), p.2377-2393

2007

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Defining functional classes of Barth syndrome mutation in humans

Human molecular genetics, 2016-05, Vol.25 (9), p.1754-1770

2016

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Mitochondria as a target of environmental toxicants

Toxicological sciences, 2013-07, Vol.134 (1), p.1-17

2013

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Fusarial Toxin–Induced Toxicity in Cultured Cells and in Isolated Mitochondria Involves PTPC-Dependent Activation of the Mitochondrial Pathway of Apoptosis

Toxicological sciences, 2009-08, Vol.110 (2), p.363-375

2009

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Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease

Human molecular genetics, 2011-12, Vol.20 (23), p.4515-4529

2011

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Hippocampal mutant APP and amyloid beta-induced cognitive decline, dendritic spine loss, defective autophagy, mitophagy and mitochondrial abnormalities in a mouse model of Alzheimer's disease

Human molecular genetics, 2018-04, Vol.27 (8), p.1332-1342

2018

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Motor neuron mitochondrial dysfunction in spinal muscular atrophy

Human molecular genetics, 2016-08, Vol.25 (16), p.3395-3406

2016

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Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics

Human molecular genetics, 2010-10, Vol.19 (19), p.3734-3746

2010

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LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease

Human molecular genetics, 2019-05, Vol.28 (10), p.1645-1660

2019

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De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment

Human molecular genetics, 2020-06, Vol.29 (9), p.1568-1579

2020

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Adipocyte Mitochondrial Function Is Reduced in Human Obesity Independent of Fat Cell Size

The journal of clinical endocrinology and metabolism, 2014-02, Vol.99 (2), p.E209-E216

2014

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Mitochondria-targeted molecules MitoQ and SS31 reduce mutant huntingtin-induced mitochondrial toxicity and synaptic damage in Huntington's disease

Human molecular genetics, 2016-05, Vol.25 (9), p.1739-1753

2016

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Mitochondria: a therapeutic target in acute kidney injury

Nephrology, dialysis, transplantation, 2016-07, Vol.31 (7), p.1062-1069

2016

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Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease

Human molecular genetics, 2023-07, Vol.32 (15), p.2441-2454

2023

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PARK2 enhancement is able to compensate mitophagy alterations found in sporadic Alzheimer's disease

Human molecular genetics, 2016-02, Vol.25 (4), p.792-806

2016

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Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction

Brain (London, England : 1878), 2021-09, Vol.144 (8), p.2471-2485

2021

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Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations

Human molecular genetics, 2020-06, Vol.29 (9), p.1547-1567

2020

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Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

Human molecular genetics, 2011-04, Vol.20 (7), p.1438-1455

2011

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Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models

Human molecular genetics, 2014-03, Vol.23 (6), p.1413-1424

2014

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Mitochondria-targeted small molecule SS31: a potential candidate for the treatment of Alzheimer's disease

Human molecular genetics, 2017-04, Vol.26 (8), p.1483-1496

2017

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The role of astrocytes in seizure generation: insights from a novel in vitro seizure model based on mitochondrial dysfunction

Brain (London, England : 1878), 2019-02, Vol.142 (2), p.391-411

2019

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The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

Human molecular genetics, 2016-07, Vol.25 (14), p.2972-2984

2016

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Axonal transport defects are a common phenotype in Drosophila models of ALS

Human molecular genetics, 2016-06, Vol.25 (12), p.2378-2392

2016

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Arsenite renal apoptotic effects in chickens co-aggravated by oxidative stress and inflammatory response

Metallomics, 2018-12, Vol.10 (12), p.1805

2018

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TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

Brain (London, England : 1878), 2022-09, Vol.145 (9), p.3095-3107

2022

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Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage

Defining functional classes of Barth syndrome mutation in humans

Mitochondria as a target of environmental toxicants

Fusarial Toxin–Induced Toxicity in Cultured Cells and in Isolated Mitochondria Involves PTPC-Dependent Activation of the Mitochondrial Pathway of Apoptosis

Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease

Hippocampal mutant APP and amyloid beta-induced cognitive decline, dendritic spine loss, defective autophagy, mitophagy and mitochondrial abnormalities in a mouse model of Alzheimer's disease

Motor neuron mitochondrial dysfunction in spinal muscular atrophy

Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics

LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment

Adipocyte Mitochondrial Function Is Reduced in Human Obesity Independent of Fat Cell Size

Mitochondria-targeted molecules MitoQ and SS31 reduce mutant huntingtin-induced mitochondrial toxicity and synaptic damage in Huntington's disease

Mitochondria: a therapeutic target in acute kidney injury

Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease

PARK2 enhancement is able to compensate mitophagy alterations found in sporadic Alzheimer's disease

Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction

Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations

Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models

Mitochondria-targeted small molecule SS31: a potential candidate for the treatment of Alzheimer's disease

The role of astrocytes in seizure generation: insights from a novel in vitro seizure model based on mitochondrial dysfunction

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations

Axonal transport defects are a common phenotype in Drosophila models of ALS

Arsenite renal apoptotic effects in chickens co-aggravated by oxidative stress and inflammatory response

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

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